Antiatherosclerotic Effect of Korean Red Ginseng Extract Involves Regulator of G-Protein Signaling 5

被引:5
作者
Im, Eun Ju [1 ]
Yayeh, Taddesse [2 ]
Park, Sang-Joon [3 ]
Kim, Seung-Hyung [4 ]
Goo, Youn-Kyoung [5 ]
Hong, Seung-Bok [6 ]
Son, Young Min [1 ]
Kim, Sung Dae [7 ]
Rhee, Man Hee [1 ]
机构
[1] Kyungpook Natl Univ, Coll Vet Med, Lab Vet Physiol & Cell Signaling, Taegu 702701, South Korea
[2] Debre Markos Univ, Coll Agr & Nat Resource, Dept Anim Sci, Debre Markos, Ethiopia
[3] Kyungpook Natl Univ, Coll Vet Med, Lab Vet Histol, Taegu 702701, South Korea
[4] Daejeon Univ, Inst Tradit Med & Biosci, Taejon 300716, South Korea
[5] Kyungpook Natl Univ, Dept Parasitol & Trop Med, Sch Med, Taegu 700422, South Korea
[6] Chungbuk Hlth & Sci Univ, Dept Clin Lab Sci, Chungbuk 363794, South Korea
[7] Dongnam Inst Radiol & Med Sci, Res Ctr, Pusan 619953, South Korea
基金
新加坡国家研究基金会;
关键词
QUALITY-OF-LIFE; STIMULATED RAW264.7 CELLS; PARKINSONS-DISEASE; ACCELERATED ATHEROSCLEROSIS; INFLAMMATION; LEPTIN; QUESTIONNAIRE; ADIPONECTIN; CONTRIBUTES; ACTIVATION;
D O I
10.1155/2014/985174
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Regulator of G-protein signaling 5 (RGS5), an inhibitor of G alpha(q) and G alpha(i) activation, has been reported to have antiatherosclerosis. Previous studies showed antiatherosclerotic effect of Korean red ginseng water extract (KRGE) via multiple signaling pathways. However, potential protective effect of KRGE through RGS5 expression has not been elucidated. Here, we investigated the antiatherosclerotic effect of KRGE in vivo and in vitro and its role on RGS5 mRNA expression. Elevated levels of total cholesterol, lactate dehydrogenase (LDH), and triglyceride (TG) in western diet groups of low-density lipoprotein receptor deficient LDLr-/- mice were reversed by oral administration of KRGE. KRGE suppressed transcriptional activity of tumor necrotic factor alpha (TNF-alpha), interleukin-6 (IL-6), and leptin in adipose tissue. It also potently repressed western diet-induced atheroma formation in aortic sinus. While KRGE showed reduced mRNA expression of inducible nitric oxide synthase (iNOS), cyclooxygenase-2 (COX-2), IL-1 beta, IL-6, and TNF-alpha in LPS-stimulated RAW264.7 cells, it enhanced mRNA expression of RGS5. Moreover, RGS5 siRNA transfection of microglia cells pretreated with KRGE reversed its inhibitory effect on the expression of iNOS, COX-2, and IL-1 beta mRNA. In conclusion, KRGE showed antiatherosclerotic and anti-inflammatory effects in western diet fed LDLr-/- mice and this effect could partly be mediated by RGS5 expression.
引用
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页数:11
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